Variant report

Variant	rs2116932
Chromosome Location	chr19:39936693-39936694
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39935867..39937651-chr19:40022035..40024212,2	MCF-7	breast:
2	chr10:110600017..110602623-chr19:39936347..39938465,2	MCF-7	breast:
3	chr19:39934545..39937545-chr19:40023023..40025430,4	MCF-7	breast:
4	chr19:39935872..39937858-chr19:40003816..40005942,2	MCF-7	breast:
5	chr1:28974685..28975549-chr19:39935889..39936794,2	Hela-S3	cervix:
6	chr19:39934091..39937114-chr19:39969895..39972879,3	K562	blood:
7	chr11:59436292..59437100-chr19:39936247..39937025,2	Hela-S3	cervix:
8	chr19:39936325..39937843-chr19:40029229..40031562,2	MCF-7	breast:
9	chr19:39934676..39937838-chr19:39970025..39973557,7	MCF-7	breast:
10	chr19:39934091..39937562-chr19:39970121..39972977,5	K562	blood:
11	chr19:39936167..39938828-chr19:39963959..39966821,3	K562	blood:
12	chr19:39933642..39937454-chr19:40029470..40032868,6	MCF-7	breast:
13	chr19:39930372..39932549-chr19:39934536..39937097,4	K562	blood:
14	chr19:39934791..39938517-chr19:40022234..40026334,4	K562	blood:
15	chr19:39831465..39834764-chr19:39935836..39937934,3	K562	blood:
16	chr19:39935972..39937694-chr19:39965602..39968199,3	K562	blood:
17	chr19:39934619..39937838-chr19:39970480..39972998,6	MCF-7	breast:
18	chr19:39936259..39938651-chr19:39958847..39961509,4	MCF-7	breast:
19	chr19:39903188..39905724-chr19:39934407..39937965,7	MCF-7	breast:
20	chr19:39924469..39929022-chr19:39934307..39938518,21	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000179134	Chromatin interaction
ENSG00000269792	Chromatin interaction
ENSG00000105197	Chromatin interaction
ENSG00000090924	Chromatin interaction
ENSG00000269584	Chromatin interaction
ENSG00000186838	Chromatin interaction
ENSG00000176401	Chromatin interaction
ENSG00000166889	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000255355	Chromatin interaction
ENSG00000269246	Chromatin interaction
ENSG00000196235	Chromatin interaction
ENSG00000176396	Chromatin interaction
ENSG00000105193	Chromatin interaction
ENSG00000130755	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10412931	0.80[ASW][hapmap];0.89[CEU][hapmap];0.95[GIH][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes]
rs10423537	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10424217	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1110627	0.80[ASW][hapmap];0.92[CEU][hapmap];0.95[GIH][hapmap];0.87[MEX][hapmap];0.98[TSI][hapmap];0.86[EUR][1000 genomes]
rs1130180	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12609112	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12978920	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12978954	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12979605	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12983040	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1529732	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1560730	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17626	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs17628	0.84[ASN][1000 genomes]
rs1865091	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1865092	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1932	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2009970	0.86[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2060270	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2060271	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2060272	0.87[EUR][1000 genomes]
rs2288933	0.86[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2288934	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2304219	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2304221	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2353678	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2353679	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs251855	0.96[CEU][hapmap];0.86[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs251856	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs251857	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs251858	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs251859	0.96[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs251860	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28528765	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28637729	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28649498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs31725	0.81[GIH][hapmap]
rs31727	0.92[CEU][hapmap];0.84[GIH][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs31728	0.92[CEU][hapmap];0.81[CHB][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34918990	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35647910	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4390710	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4802026	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4803237	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4803240	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4803241	0.85[CHB][hapmap];0.86[JPT][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4803242	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4803245	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4803246	0.86[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4803247	0.86[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4803250	0.83[EUR][1000 genomes]
rs480595	0.84[ASN][1000 genomes]
rs480656	0.84[ASN][1000 genomes]
rs481421	0.91[CHB][hapmap];0.84[CHD][hapmap];0.84[ASN][1000 genomes]
rs504017	0.84[ASN][1000 genomes]
rs530411	0.95[CHB][hapmap];0.86[CHD][hapmap];0.86[ASN][1000 genomes]
rs564577	0.96[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.93[TSI][hapmap]
rs566130	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59007555	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs640000	0.84[ASN][1000 genomes]
rs6508862	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6508863	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6508864	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6508865	0.90[EUR][1000 genomes]
rs651601	0.91[CHB][hapmap];0.86[CHD][hapmap];0.83[ASN][1000 genomes]
rs686956	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7251384	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7251652	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7255253	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7257526	0.80[ASW][hapmap];0.87[MEX][hapmap];0.88[TSI][hapmap]
rs73035416	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73549933	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8107194	0.86[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.96[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8107647	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8110134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8110716	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8111260	0.92[EUR][1000 genomes]
rs878754	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870133	chr19:39822160-39938468	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
2	nsv911685	chr19:39888449-39948779	Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	222 gene(s)	inside rSNPs	diseases
3	nsv911689	chr19:39903088-40021759	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv911690	chr19:39903088-40046863	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv523856	chr19:39913558-39997472	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	esv1791966	chr19:39921479-39954931	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs2116932	B3GNT8	cis	parietal	SCAN
rs2116932	RPS16	cis	lymphoblastoid	seeQTL
rs2116932	RPS16	Cis_1M	lymphoblastoid	RTeQTL
rs2116932	C19orf61	cis	cerebellum	SCAN
rs2116932	NUMBL	cis	parietal	SCAN
rs2116932	GRIK5	cis	parietal	SCAN
rs2116932	BCAM	cis	parietal	SCAN
rs2116932	RPS16	cis	multi-tissue	Pritchard
rs2116932	RPS16	cis	Lymphoblastoid	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39934800-39937000	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr19:39934800-39937000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr19:39934800-39937000	Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr19:39934800-39937000	Active TSS	A549	lung
5	chr19:39934800-39937200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:39935000-39936800	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr19:39935000-39936800	Active TSS	Muscle Satellite Cultured Cells	--
8	chr19:39935000-39936800	Active TSS	HMEC	breast
9	chr19:39935000-39936800	Active TSS	NHEK	skin
10	chr19:39935000-39937000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr19:39935000-39937000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr19:39935000-39937000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr19:39935000-39937000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:39935000-39937000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:39935000-39937000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:39935000-39937000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr19:39935000-39937000	Active TSS	Psoas Muscle	Psoas
18	chr19:39935000-39937000	Active TSS	Rectal Smooth Muscle	rectum
19	chr19:39935000-39937000	Active TSS	Right Ventricle	heart
20	chr19:39935000-39937200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr19:39935000-39937400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr19:39935000-39937400	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr19:39935000-39937400	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr19:39935000-39937400	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr19:39935000-39937600	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr19:39935200-39936800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr19:39935200-39936800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr19:39935200-39936800	Active TSS	Primary T cells from cord blood	blood
29	chr19:39935200-39936800	Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr19:39935200-39936800	Active TSS	Brain Cingulate Gyrus	brain
31	chr19:39935200-39936800	Active TSS	Brain Hippocampus Middle	brain
32	chr19:39935200-39936800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr19:39935200-39936800	Active TSS	Colon Smooth Muscle	Colon
34	chr19:39935200-39936800	Active TSS	Fetal Lung	lung
35	chr19:39935200-39937000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr19:39935200-39937000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:39935200-39937000	Active TSS	Aorta	Aorta
38	chr19:39935200-39937000	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr19:39935200-39937000	Active TSS	Esophagus	oesophagus
40	chr19:39935200-39937000	Active TSS	Fetal Muscle Trunk	muscle
41	chr19:39935200-39937000	Active TSS	Gastric	stomach
42	chr19:39935200-39937000	Active TSS	Left Ventricle	heart
43	chr19:39935200-39937000	Active TSS	Placenta Amnion	Placenta Amnion
44	chr19:39935200-39937000	Bivalent/Poised TSS	HepG2	liver
45	chr19:39935200-39937000	Active TSS	K562	blood
46	chr19:39935200-39937000	Active TSS	NHDF-Ad	bronchial
47	chr19:39935200-39937000	Active TSS	NHLF	lung
48	chr19:39935200-39937200	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr19:39935200-39937200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr19:39935200-39937200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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